Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_provenance.
- NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_assertion description "[Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_provenance.
- NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_assertion evidence source_evidence_curated NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_provenance.
- NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_assertion SIO_000772 23793026 NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_provenance.
- NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_assertion wasDerivedFrom ctd_human-2016 NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_provenance.
- NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_assertion wasGeneratedBy ECO_0000218 NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP33114.RAp7Sdo9p0eNzJnYiFQYByFcOHKMp5xthXWiyW4Nm32UI130_provenance.